OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION— 510(k) K880263

Name: FDA 510(k) clearance K880263
Creator: U.S. Food and Drug Administration
Published: 1988-03-15

Substantially Equivalent

Orthopedic Systems, Inc.

FDA 510(k) clearance K880263 for OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION, Substantially Equivalent on 1988-03-15. Applicant: Orthopedic Systems, Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Systems, Inc.
Product code: Code JEB
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1988-01-22
Decision date: 1988-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hayward, CA, US

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